Team:BostonU/Results

From 2013.igem.org

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<br>This summer, we created and submitted 59 new Level 0 Parts, 17 new Destination Vectors, and 29 new Level 1 Transcriptional Units to the <a href="https://2013.igem.org/Team:BostonU/Parts">MoClo Library</a>  
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<br><p>This summer, we created and submitted 59 new Level 0 Parts, 17 new Destination Vectors, and 29 new Level 1 Transcriptional Units to the <a href="https://2013.igem.org/Team:BostonU/Parts">MoClo Library</a></p>
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<br>We have also updated the <a href="https://2013.igem.org/Team:BostonU/MoClo">MoClo Kit</a> to include 87 Level 0 Basic Parts and 28 Destination Vectors so teams next year can create devices containing up to 4 transcriptional units
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<br><p>We have also updated the <a href="https://2013.igem.org/Team:BostonU/MoClo">MoClo Kit</a> to include 87 Level 0 Basic Parts and 28 Destination Vectors so teams next year can create devices containing up to 4 transcriptional units</p>
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<br>Using a state of the art BD LSRFortessa at the Center of Synthetic Biology here at Boston University, we have successfully <a href="https://2013.igem.org/Team:BostonU/Data">characterized</a> 64 Level 1 Transcriptional Units and 2 Level 2 Devices
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<br><p>Using a state of the art BD LSRFortessa at the Center of Synthetic Biology here at Boston University, we have successfully <a href="https://2013.igem.org/Team:BostonU/Data">characterized</a> 64 Level 1 Transcriptional Units and 2 Level 2 Devices</p>
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<br>From this work, we have drafted a proposal for a standardized flow cytometry protocol for future teams to utilize when testing devices containing fluorescent proteins in <i>E. coli</i>
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<br><p>From this work, we have drafted a proposal for a standardized flow cytometry protocol for future teams to utilize when testing devices containing fluorescent proteins in <i>E. coli</i></p>
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<br>Working closely with the <a href="https://2013.igem.org/Team:Purdue">Purdue Biomakers</a> team, we are designing a <a href="https://2013.igem.org/Team:BostonU/DataSheet">data sheet</a> that will allow users to more easily share information and data within the iGEM community and beyond
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<br><p>Working closely with the <a href="https://2013.igem.org/Team:Purdue">Purdue Biomakers</a> team, we are designing a <a href="https://2013.igem.org/Team:BostonU/DataSheet">datasheet</a> that will allow users to more easily share information and data within the iGEM community and beyond</p>
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<br>We have begun implementing a Java-based web tool to generate these data sheets
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<br><p>We have begun implementing a Java-based web tool to generate these data sheets</p>
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Revision as of 03:34, 27 September 2013



Results Summary

Below is a brief summary of our results from this summer. Each statement has a link shown in RED to the page(s) containing more information and detailed results.




      This summer, we created and submitted 59 new Level 0 Parts, 17 new Destination Vectors, and 29 new Level 1 Transcriptional Units to the MoClo Library



      We have also updated the MoClo Kit to include 87 Level 0 Basic Parts and 28 Destination Vectors so teams next year can create devices containing up to 4 transcriptional units




      Using a state of the art BD LSRFortessa at the Center of Synthetic Biology here at Boston University, we have successfully characterized 64 Level 1 Transcriptional Units and 2 Level 2 Devices



      From this work, we have drafted a proposal for a standardized flow cytometry protocol for future teams to utilize when testing devices containing fluorescent proteins in E. coli




      Working closely with the Purdue Biomakers team, we are designing a datasheet that will allow users to more easily share information and data within the iGEM community and beyond



      We have begun implementing a Java-based web tool to generate these data sheets